The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126712721 12671272 1 I 201510 20151230 20160822 20160822 PER US-TEVA-623219USA TEVA 57.77 YR F Y 85.71000 KG 20160822 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126712721 12671272 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; 4FR0197 (43F012) 76191 180 MG TABLET QD
126712721 12671272 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 360 MILLIGRAM DAILY; 4FR0197 (43F012) 76191 180 MG TABLET BID
126712721 12671272 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; 4FR0197 (43F012) 76191 180 MG TABLET QD
126712721 12671272 4 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 4FR0197 (43F012) 76191
126712721 12671272 5 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 4FR0197 (43F012) 76191

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126712721 12671272 1 Hypersensitivity
126712721 12671272 2 Rhinorrhoea
126712721 12671272 3 Throat irritation
126712721 12671272 4 Pruritus
126712721 12671272 5 Dry skin

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126712721 12671272 Drug ineffective
126712721 12671272 Incorrect dose administered
126712721 12671272 Off label use

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126712721 12671272 1 201510 201512 0
126712721 12671272 2 201512 201512 0
126712721 12671272 3 201512 20151229 0